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Correlation of microsomal antibodies with the intensity of the intrathyroidal autoimmune process in Graves' disease.
- Source :
-
The Journal of clinical endocrinology and metabolism [J Clin Endocrinol Metab] 1993 Oct; Vol. 77 (4), pp. 939-43. - Publication Year :
- 1993
-
Abstract
- Graves' disease is an organ-specific autoimmune disease, and intrathyroidal lymphocytes seem to be the major source of thyroid autoantibodies. Consequently, the intensity of the intrathyroidal lymphocytic infiltration is generally believed to reflect the activity of the autoimmune process. We, therefore, investigated the correlation of microsomal (enzyme immunoassay), thyroglobulin (RIA), and TSH receptor antibodies (RRA) with the degree of intrathyroidal infiltration by immunoglobulin G-producing plasma cells, activated T-cells, antigen-presenting cells, and the total number of lymphocytes. The immunocompetent cells were identified immunohistologically with monoclonal antibodies for immunoglobulins kappa and lambda, UCHL1, and the S100 antibody, respectively, in 26 thyroid glands of patients suffering from Graves' disease. The intensity of lymphocytic infiltration was determined by the point-counting method and by counting all lymphocytes and the labeled lymphocytes in 3 x 51 visual fields or 3 slides/thyroid gland. Microsomal antibodies correlated significantly (P = 0.001) with the total number of lymphocytes (r = 0.86), kappa (r = 0.71), lambda (r = 0.71), UCHL1 (r = 0.9), and S100 (r = 0.9) positive cells. These correlations were also significant for thyroglobulin antibodies. However, TSH receptor antibodies showed no significant correlations with any of the populations of immunocompetent cells. Patients with preoperatively undetectable TSH receptor or microsomal antibodies showed a broad variation of intrathyroidal infiltration by the immunocompetent cells investigated. Microsomal antibody titers, therefore, seem to reflect the intensity of the intrathyroidal autoimmune process in Graves' disease better than TSH receptor antibodies. However, the broad baseline variation in intrathyroidal infiltration observed with nondetectable thyroid antibodies will not always allow determination of the intensity of the intrathyroidal autoimmune process from microsomal or thyroglobulin antibody titers.
- Subjects :
- Adult
Antigen-Presenting Cells immunology
Autoimmune Diseases drug therapy
Autoimmune Diseases pathology
Carbimazole therapeutic use
Graves Disease drug therapy
Graves Disease pathology
Humans
Immunoglobulin kappa-Chains biosynthesis
Immunoglobulin lambda-Chains biosynthesis
Lymphocytes immunology
Plasma Cells immunology
Propylthiouracil therapeutic use
Receptors, Thyrotropin immunology
T-Lymphocytes immunology
Thyroglobulin antagonists & inhibitors
Thyrotropin biosynthesis
Autoantibodies biosynthesis
Autoimmune Diseases immunology
Graves Disease immunology
Microsomes immunology
Thyroid Gland immunology
Subjects
Details
- Language :
- English
- ISSN :
- 0021-972X
- Volume :
- 77
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- The Journal of clinical endocrinology and metabolism
- Publication Type :
- Academic Journal
- Accession number :
- 8408468
- Full Text :
- https://doi.org/10.1210/jcem.77.4.8408468